Overall Survival with Brentuximab Vedotin in Stage III or IV Hodgkin's Lymphoma

被引:179
|
作者
Ansell, Stephen M. [1 ]
Radford, John [2 ,3 ]
Connors, Joseph M. [4 ]
Dlugosz-Danecka, Monika [5 ]
Kim, Won-Seog [7 ]
Gallamini, Andrea [9 ]
Ramchandren, Radhakrishnan [10 ]
Friedberg, Jonathan W. [11 ]
Advani, Ranjana [13 ]
Hutchings, Martin [14 ]
Evens, Andrew M. [15 ]
Smolewski, Piotr [6 ]
Savage, Kerry J. [4 ]
Bartlett, Nancy L. [16 ]
Eom, Hyeon-Seok [8 ]
Abramson, Jeremy S. [17 ]
Dong, Cassie [18 ]
Campana, Frank [18 ]
Fenton, Keenan [19 ]
Puhlmann, Markus [19 ]
Straus, David J. [12 ]
机构
[1] Mayo Clin, Div Hematol, Rochester, MN 55905 USA
[2] Univ Manchester, Manchester, Lancs, England
[3] Christie NHS Fdn Trust, Manchester Acad Hlth Sci Ctr, Manchester, Lancs, England
[4] BC Canc Ctr Lymphoid Canc, Vancouver, BC, Canada
[5] Maria Sklodowska Curie Natl Res Inst Oncol, Krakow, Poland
[6] Med Univ Lodz, Dept Expt Hematol, Lodz, Poland
[7] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Div Hematol Oncol,Dept Internal Med, Seoul, South Korea
[8] Natl Canc Ctr, Ctr Hematol Malignancy, Dept Hematol Oncol, Goyang, South Korea
[9] Antoine Lacassagne Canc Ctr, Res & Innovat Dept, Nice, France
[10] Univ Tennessee, Grad Sch Med, Knoxville, TN USA
[11] Univ Rochester, Wilmot Canc Inst, Rochester, MN USA
[12] Mem Sloan Kettering Canc Ctr, Dept Med, Lymphoma Serv, 1275 York Ave, New York, NY 10021 USA
[13] Stanford Univ, Div Oncol, Dept Med, Stanford, CA 94305 USA
[14] Copenhagen Univ Hosp, Dept Hematol, Rigshosp, Copenhagen, Denmark
[15] Rutgers Canc Inst New Jersey, Div Blood Disorders, New Brunswick, NJ USA
[16] Washington Univ, Sch Med, Siteman Canc Ctr, St Louis, MO 63110 USA
[17] Massachusetts Gen Hosp, Boston, MA 02114 USA
[18] Takeda Dev Ctr Amer, Lexington, KY USA
[19] Seagen, Bothell, WA USA
关键词
OPEN-LABEL; CHEMOTHERAPY; ABVD; COMBINATION; TOMOGRAPHY; INTERGROUP; THERAPY; BEACOPP; DISEASE; CYCLES;
D O I
10.1056/NEJMoa2206125
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Five-year follow-up in a trial involving patients with previously untreated stage III or IV classic Hodgkin's lymphoma showed long-term progression-free survival benefits with first-line therapy with brentuximab vedotin, a CD30-directed antibody-drug conjugate, plus doxorubicin, vinblastine, and dacarbazine (A+AVD), as compared with doxorubicin, bleomycin, vinblastine, and dacarbazine (ABVD). A planned interim analysis indicated a potential benefit with regard to overall survival; data from a median of 6 years of follow-up are now available. METHODS We randomly assigned patients in a 1:1 ratio to receive up to six cycles of A+AVD or ABVD. The primary end point, modified progression-free survival, has been reported previously. The key secondary end point was overall survival in the intention-to-treat population. Safety was also assessed. RESULTS A total of 664 patients were assigned to receive A+AVD and 670 to receive ABVD. At a median follow-up of 73.0 months, 39 patients in the A+AVD group and 64 in the ABVD group had died (hazard ratio, 0.59; 95% confidence interval [CI], 0.40 to 0.88; P=0.009). The 6-year overall survival estimates were 93.9% (95% CI, 91.6 to 95.5) in the A+AVD group and 89.4% (95% CI, 86.6 to 91.7) in the ABVD group. Progression-free survival was longer with A+AVD than with ABVD (hazard ratio for disease progression or death, 0.68; 95% CI, 0.53 to 0.86). Fewer patients in the A+AVD group than in the ABVD group received subsequent therapy, including transplantation, and fewer second cancers were reported with A+AVD (in 23 vs. 32 patients). Primary prophylaxis with granulocyte colony-stimulating factor was recommended after an increased incidence of febrile neutropenia was observed with A+AVD. More patients had peripheral neuropathy with A+AVD than with ABVD, but most patients in the two groups had resolution or amelioration of the event by the last follow-up. CONCLUSION Patients who received A+AVD for the treatment of stage III or IV Hodgkin's lymphoma had a survival advantage over those who received ABVD.
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收藏
页码:310 / 320
页数:11
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